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MODIFICATION TO ACUSON X300 ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071036
510(k) Type
Special
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/2007
Days to Decision
34 days
Submission Type
Summary

MODIFICATION TO ACUSON X300 ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071036
510(k) Type
Special
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/2007
Days to Decision
34 days
Submission Type
Summary